Use of azetidinone compounds

ABSTRACT

The use of azetidinone compounds that are inhibitors of cholesterol absorption as tools for discovering and characterizing proteins involved in trafficking or absorption of cholesterol and/or cholesteryl esters in biological systems is presented These compounds can serve as tools for competitive binding assays to discover and characterize other chemical agents useful as cholesterol absorption inhibitors. New compounds of the present invention are also highly efficacious inhibitors of cholesterol absorption.

This application is a continuation of co-pending U.S. application Ser.No. 11/1123,615, filed May 6, 2005, now U.S. Pat. No. 7,144,696, whichis a divisional of U.S. application Ser. No. 10/438,637, filed May 1512003, now U.S. Pat. No. 6,933,107, which is a divisional of U.S.application Ser. No. 09/547,509, filed Apr. 12, 2000, now U.S. Pat. No.6,593,078, which claims priority under 35 U.S.C. §119(e) to U.S.application Ser. No. 60/129,610, filed Apr. 16, 1999, now abandoned,each of which are herein incorporated by reference in their entireties.

FIELD OF THE INVENTION

The present invention relates to the use of azetidinone compounds thatare inhibitors of cholesterol absorption as tools for discovering andcharacterizing proteins involved in trafficking or absorption ofcholesterol and/or cholesteryl esters in biological systems. Further,these compounds can serve as tools for competitive binding assays todiscover and characterize other chemical agents useful as cholesterolabsorption inhibitors. New compounds of the present invention are highlyefficacious inhibitors of cholesterol absorption.

BACKGROUND OF THE INVENTION

Atherosclerotic coronary heart disease (CHD) represents the major causefor death and cardiovascular morbidity in the western world. Riskfactors for CHD include hypertension, diabetes mellitus, family history,male gender, cigarette smoke and serum cholesterol. A total cholesterollevel in excess of 225 to 250 mg/dl is associated with significantelevation of risk of CHD.

Cholesteryl esters are a major component of atherosclerotic lesions andthe major storage form of cholesterol in arterial wall cells. Formationof cholesteryl esters is also a key step in the intestinal absorption ofdietary cholesterol. Thus, inhibition of cholesteryl ester formation andreduction of serum cholesterol is likely to inhibit the progression ofatherosclerotic lesion formation, decrease the accumulation ofcholesteryl esters in the arterial wall, and block the intestinalabsorption of dietary cholesterol.

The regulation of whole-body cholesterol homeostasis in humans andanimals involves the regulation of dietary cholesterol and modulation ofcholesterol biosynthesis, bile acid biosynthesis and the catabolism ofthe cholesterol-containing plasma lipoproteins. The liver is the majororgan responsible for cholesterol biosynthesis and catabolism and forthis reason, it is a prime determinant of plasma cholesterol levels. Theliver is the site of synthesis and secretion of very low densitylipoproteins (VLDL) which are subsequently metabolized to low densitylipoproteins (LDL) in the circulation. LDL are the predominantcholesterol-carrying lipoproteins in the plasma and an increase in theirconcentration is correlated with increased atherosclerosis.

When intestinal cholesterol absorption is reduced, by whatever means,less cholesterol is delivered to the liver. The consequence of thisaction is decreased hepatic lipoprotein production, and an increase inthe hepatic clearance of plasma cholesterol, mostly as LDL. Thus, thenet effect of inhibiting intestinal cholesterol absorption is a decreasein plasma cholesterol levels.

Certain azetidinone core structures have been reported to be useful inlowering cholesterol levels by decreasing intestinal cholesterolabsorption. These related azetidinone cores and their synthesis aredetailed in the following commonly assigned United States patents, thedisclosures of which are incorporated, in their entirety, herein byreference: U.S. Pat. Nos. 5,688,787; 5,698,548; 5,624,920; 5,631,365;5,633,246; 5,656,624; 5,744,467; and 5,767,115. The discovery of2-azetidinones as potent and selective intestinal cholesterol absorptioninhibitors has confirmed this mechanism as a key point of interventionfor lowering cholesterol plasma levels and has validated the therapeuticvalue of such an approach. The mechanism by which cholesterol moves fromthe lumen into the epithelial layer lining the small intestine is notwell understood. Recent experimental evidence supports the notion of anactive transport process mediated by a protein or proteins in theenterocyte brush border membrane rather than a simple diffusion model.Kinetic analysis and sterol specificity of cholesterol uptake as well asthe structure-activity relationship studies of the cholesterolabsorption inhibitors are consistent with a specific proteinreceptor/transporter regulated event. Potential molecules for thisprocess have been proposed in recent years. However, the specificbiochemical pathway responsible for cholesterol absorption remains to bedefined.

Compounds I and II (especially II)

where R is fluorine, are potent inhibitors of cholesterol uptake inanimal models and humans. The mechanism by which these compounds andrelated 2-azetidinones inhibit the uptake of cholesterol across theintestinal wall is not known. These compounds do not sequester bileacids or precipitate cholesterol Nor do they potently inhibit HMG-CoAreductase, pancreatic lipase, or acyl-CoA cholesterol acyl transferase(ACAT). Understanding the mechanism by which these compounds inhibitcholesterol absorption will shed light on the biochemical pathwaysinvolved in the uptake of dietary and biliary cholesterol.

SUMMARY OF THE INVENTION

In one aspect, this invention provides a method for identifying aprotein involved in cholesterol absorption in a biological system, themethod comprising the steps of: (a) providing a cDNA expression librarycapable of expressing a protein involved in cholesterol absorption in abiological system, said cDNA expression library comprising a pluralityof cells capable of expressing different cDNAs; (b) screening saidexpression library by incubating cells from said library with afluorescent cholesterol absorption inhibitor; (c) after step (b),identifying the cell or cells in said library that display the greatestamount of fluorescence; and (d) identifying the protein associated withthe cDNA expressed by said cell or cells displaying the greatest amountof fluorescence.

In another aspect, this invention provides a method for assayinginhibitory agents for activity against cholesterol absorption, themethod comprising the steps of: providing a cell capable of binding afluorescent cholesterol absorption inhibitor; contacting said cell witha candidate inhibitory agent in the presence of said fluorescentcholesterol absorption inhibitor; and measuring the inhibition of thefluorescence of said cell.

In still another aspect, this invention provides a method foridentifying inhibitory agents which inhibit the absorption ofcholesterol into a cell membrane, said method comprising the steps of:(a) combining a fluorescent cholesterol absorption inhibitor, said cellmembrane and a candidate inhibitory agent, under conditions wherein, butfor the presence of said inhibitory agent, said fluorescent cholesterolabsorption inhibitor is bound to the membrane; and (b) detecting therelative presence or absence of fluorescent cholesterol absorptioninhibitor absorption bound to the membrane, wherein a relative absenceof fluorescent cholesterol absorption inhibitor absorption indicatesthat said candidate inhibitory agent is an inhibitory agent whichinhibits cholesterol absorption into the membrane.

In another aspect, this invention provides a method for identifyinginhibitory agents which inhibit the absorption of cholesterol, saidmethod comprising the steps oft (a) combining a labeled cholesterolabsorption inhibitor, a cell expressing the scavenger receptor type B,class I (SR-SI) and a candidate inhibitory agent, under conditionswherein, but for the presence of said inhibitory agent, said labeledcholesterol absorption inhibitor binds to SR-BI; and (b) detecting therelative presence or absence of labeled cholesterol absorption inhibitorabsorption bound to SR-BI wherein a relative absence of labeledcholesterol absorption inhibitor absorption indicates that saidcandidate inhibitory agent is an inhibitory agent which inhibitsSR-BI-mediated cellular cholesterol absorption.

In further aspects, this invention provides proteins and new inhibitoryagents identified by the above methods. This invention also providesnovel fluorescent cholesterol absorption inhibitors of formulas I andII:

wherein R comprises a fluorescent moiety.

DETAILED DESCRIPTION OF THE INVENTION

A. Novel Fluorescent Cholesterol Absorption Inhibitors

Novel fluorescent cholesterol absorption inhibitors of this inventioninclude compounds of formulas I and II:

wherein R comprises a fluorescent moiety. In preferred embodiments, R isa fluorescent moiety linked by an alkynyl-containing tether group. In aparticularly preferred embodiment, R is selected from the groupconsisting of:

Modification with fluorescent moieties A-B of the N-aryl ring of otherazetidinone cholesterol absorption inhibitor core structures related tothe above are contemplated as being within the scope of this inventionas well. These related azetidinone cores and their synthesis aredetailed in the following commonly assigned U.S. patents the disclosuresof which are incorporated, in their entirety, herein by reference: U.S.Pat. Nos. 5,688,787; 5,698,548; 5,624,920; 5,631,365; 5,633,246;5,656,624; 5,744,467; and 5,767,115.

Compounds in the following text are designated as:

The synthetic route to these fluorescent azetidinones is shown inScheme 1. The fluorescent alkynyl compounds are prepared fromcommercially available electrophilic fluorescent derivatives (seeHandbook of Fluorescent Probes and Research Chemicals, Molecular Probes,Inc.) and propargyl amine. The syntheses of N-iodophenyl azetidinonederivatives have been described in previous patents, cited above. Thefluorescent alkynylated material is then coupled to theN-iodophenylazetidinone via a palladium mediated coupling reactionDeprotection of the glucuronide ester is accomplished as a final step inanalogs bearing this moiety.

B. General Methods

The practice of the present invention generally employs conventionaltechniques of molecular biology, microbiology, recombinant DNA, andimmunology, which are within the skill of the art. Such techniques areexplained fully in the literature. See for example J. Sambrook et al,“Molecular Cloning; A Laboratory Manual (1989); “DNA Cloning”Vol. I andII (D. N. Clover ed. 1985); “Oligonucleotide Synthesis” (M. J. Gait ed,1984); “Nucleic Acid Hybridization” (S. D. Hames & S. J. Higgins eds.1984); “Transcription And Translation” (B. D. Hames & S. J. Higgins eds.1984); “Animal Cell Culture” (R. I. Freshney ed. 1986); “ImmobilizedCells And Enzymes” (IRL Press, 1986); B. Perbal, “A Practical Guide ToMolecular Cloning” (1984); the series, “Methods In Enzymology” (AcademicPress, Inc.); “Gene Transfer Vectors For Mammalian Cells” (J. H. Millerand M. P. Calos eds. 1987, Cold Spring Harbor Laboratory); Meth Enzymol(1987) 154 and 155 (Wu and Grossman, and Wu, eds., respectively); Mayer& Walker, eds. (1987), “Immunochemical Methods In Cell And MolecularBiology” (Academic Press, London); Scopes, “Protein Purification:Principles And Practice”, 2nd Ed (Springer-Verlag, N.Y., 1987), and“Handbook Of Experimental Immunology”, volumes I-IV (Weir and Blackwell,eds, 1986).

C. Methods of Screening cDNA Libraries

cDNA libraries containing genes capable of expressing a protein involvedin cholesterol absorption are prepared by standard techniques, such asdescrbed in the above references. Both prokaryotic and eukaryotic hostcells are useful for expressing desired coding sequences whenappropriate control sequences compatible with the designated host areused. Among prokaryotic hosts, E. coli is most frequently used.Expression control sequences for prokaryotes include promoters,optionally containing operator portions, and ribosome binding sites.Transfer vectors compatible with prokaryotic hosts are commonly derivedfrom, for example, pBR322, a plasmid containing operons conferringampicillin and tetracycline resistance, and the various pUC vectors,which also contain sequences conferring antibiotic resistance markers.These plasmids are commercially available. The markers may be used toobtain successful transformants by selection. Commonly used prokaryoticcontrol sequences include the β-lactamase (penicillinase) and lactosepromoter systems (Chang et al, Nature (1977) 198:1056), the tryptophan(trp) promoter system (Goeddel et al, Nuc Acids Res (1980) 8:4057) andthe lambda-derived P_(L) promoter and N gene ribosome binding site(Shimatake et al, Nature (1981) 292:128) and the hybrid tac promoter (DeBoer et al, Proc Nat Acad Sci USA (1983) 292:128) derived from sequencesof the trp and lac UV5 promoters. The foregoing systems are particularlycompatible with E. coli; if desired, other prokaryotic hosts such asstrains of Bacillus or Pseudomonas may be used, with correspondingcontrol sequences.

Eukaryotic hosts include without limitation yeast and mammalian cells inculture systems. Yeast expression hosts include Saccharomyces,Klebsiella, Picia, and the like. Saccharomyces cerevisiae andSaccharomyces carlsbergensis and K. lactis are the most commonly usedyeast hosts, and are convenient fungal hosts. Yeast-compatible vectorscarry markers which permit selection of successful transformants byconferring prototrophy to auxotrophic mutants or resistance to heavymetals on wild-type strains. Yeast compatible vectors may employ the 2 μorigin of replication (Broach et al, Meth Enzymol (1983) 101:307), thecombination of CEN3 and ARS1 or other means for assuring replication,such as sequences which will result in incorporation of an appropriatefragment into the host cell genome. Control sequences for yeast vectorsare known in the art and include promoters for the synthesis ofglycolytic enzymes (Hess et al, J Adv Enzyme Reg (1968) 7:149; Hollandet al, Biochem (1978), 17:4900), including the promoter for3-phosphoglycerate kinase (R. Hitzeman et al, J Biol Chem (1980)255:2073). Terminators may also be included, such as those derived fromthe enolase gene (Holland, J Biol Chem (1981) 256:1385). Particularlyuseful control systems are those which comprise the glyceraldehyde-3phosphate dehydrogenase (GAPDH) promoter or alcohol dehydrogenase (ADH)regulatable promoter, terminators also derived from GAPDH, and ifsecretion is desired, a leader sequence derived from yeast alpha-factor(see U.S. Pat. No. 4,870,008, incorporated herein by reference).

In addition, the transcriptional regulatory region and thetranscriptional initiation region which are operably linked may be suchthat they are not naturally associated in the wild-type organism. Thesesystems are described in detail in EPO 120,551, published Oct. 3, 1984;EPO 116,201, published Aug. 22, 1984; and EPO 164,556, published Dec.18, 1985, all of which are hereby incorporated herein by reference infull.

Mammalian cell lines available as hosts for expression are known in theart and include many immortalized cell lines available from the AmericanType Culture Collection (ATCC), including HeLa cells, Chinese hamsterovary (CHO) cells, baby hamster kidney (BHK) cells, and a number ofother cell lines. Suitable promoters for mammalian cells are also knownin the art and include vital promoters such as that from Simian Virus 40(SV40) (Fiers et al, Nature (1978) 273:113), Rous sarcoma virus (RSV),adenovirus (ADV), and bovine papilloma virus (BPV). Mammalian cells mayalso require terminator sequences and poly-A addition sequences.Enhancer sequences which increase expression may also be included, andsequences which promote amplification of the gene may also be desirable(for example methotrexate resistance genes). These sequences are knownin the art.

Vectors suitable for replication in mammalian cells are known in theart, and may include vital replicons, or sequences which insureintegration of the appropriate sequences into the host genome. Forexample, another vector used to express foreign DNA is Vaccinia virus.In this case the heterologous DNA is inserted into the Vaccinia genome.Techniques for the insertion of foreign DNA into the vaccinia virusgenome are known in the art, and may utilize, for example, homologousrecombination. The heterologous DNA is generally inserted into a genewhich is non-essential to the virus, for example, the thymidine kinasegene (tk), which also provides a selectable marker. Plasmid vectors thatgreatly facilitate the construction of recombinant viruses have beendescribed (see, for example, Mackett et al, J Virol (1984) 49:857;Chakrabarti et al, Mol Cell Biol (1985) 5:3403; Moss, in GENE TRANSFERVECTORS FOR MAMMALIAN CELLS (Miller and Calos, eds., Cold Spring HarborLaboratory, N.Y., 1987), p. 10). Expression of the polypeptide thenoccurs in cells or animals which are infected with the live recombinantvaccinia virus.

Transformation may be by any known method for introducingpolynucleotides into a host cell, including, for example packaging thepolynucleotide in a virus and transducing a host cell with the virus,and by direct uptake of the polynucleotide. The transformation procedureused depends upon the host to be transformed. Bacterial transformationby direct uptake generally employs treatment with calcium or rubidiumchloride (Cohen, Proc Nat Acad Sci USA (1972) 69:2110; T. Maniatis etat, “Molecular Cloning; A Laboratory Manual” (Cold Spring Harbor Press,Cold Spring Harbor, N.Y., 1982). Yeast transformation by direct uptakemay be carried out using the method of Hinnen et al, Proc Nat Acad SciUSA (1978) 75:1929. Mammalian transformations by direct uptake may beconducted using the calcium phosphate precipitation method of Graham andVan der Eb, Virol (1 978) 52:546, or the various known modificationsthereof. Other methods for introducing recombinant polynucleotides intocells, particularly into mammalian cells, include dextran-mediatedtransfection, calcium phosphate mediated transfection, polybrenemediated transfection, protoplast fusion, electroporation, encapsulationof the polynucleotide(s) in liposomes, and direct microinjection of thepolynucleotides into nuclei.

Vector construction employs techniques which are known in the art,Site-specific DNA cleavage is performed by treating with suitablerestriction enzymes under conditions which generally are specified bythe manufacturer of these commercially available enzymes. In general,about 1 μg of plasmid or DNA sequence is cleaved by 1 unit of enzyme inabout 20 μL buffer solution by incubation for 1-2 hr at 37° C. Afterincubation with the restriction enzyme, protein is removed byphenol/chloroform extraction and the DNA recovered by precipitation withethanol. The cleaved fragments may be separated using polyacrylamide oragarose gel electrophoresis techniques, according to the generalprocedures described in Meth Enzymol (1980) 65:499-560.

Sticky-ended cleavage fragments may be blunt ended using E. coli DNApolymerase I (Klenow fragment) with the appropriate deoxynucleotidetriphosphates (dNTPs) present in the mixture. Treatment with S1 nucleasemay also be used, resulting in the hydrolysis of any single stranded DNAportions.

Ligations are carried out under standard buffer and temperatureconditions using T4 DNA ligase and ATP; sticky end ligations requireless ATP and less ligase than blunt end ligations. When vector fragmentsare used as part of a ligation mixture, the vector fragment is oftentreated with bacterial alkaline phosphatase (BAP) or calf intestinalalkaline phosphatase to remove the 5′-phosphate, thus preventingreligation of the vector. Alternatively, restriction enzyme digestion ofunwanted fragments can be used to prevent ligation. Ligation mixturesare transformed into suitable cloning hosts, such as E. coli, andsuccessful transformants selected using the markers incorporated (e.g.,antibiotic resistance), and screened for the correct construction.

Synthetic oligonucleotides may be prepared using an automatedoligonucleotide synthesizer as described by Warner, DNA (1984) 3:401. Ifdesired, the synthetic strands may be labeled with ³²P by treatment withpolynucleotide kinase in the presence of ³²P-ATP under standard reactionconditions.

For routine vector constructions, ligation mixtures are transformed intoE. coli strain HB101 or other suitable hosts, and successfultransformants selected by antibiotic resistance or other markers.Plasmids from the transformants are then prepared according to themethod of Clewell et al, Proc Nat Acad Sci USA (1969) 62:1159, usuallyfollowing chloramphenicol amplification (Clewell, J Bacteriol (1972)110:667). The DNA is isolated and analyzed, usually by restrictionenzyme analysis and/or sequencing. Sequencing may be performed by thedideoxy method of Sanger et at, Proc Nat Acad Sci USA (1977) 74:5463, asfurther described by Messing et at, Nuc Acids Res (1981) 9:309, or bythe method of Maxam et at, Meth Enzymol (1980) 65:499. Problems withband compression, which are sometimes observed in GC-rich regions, wereovercome by use of T-deazoguanosine according to Barr et al,Biotechniques (1986) 4:428.

Preferably, the cDNA libraries used in this invention are derived fromthe mRNA of cells or cell lines known to be involved in cholesterolabsorption. In a preferred embodiment of this invention, the cDNAlibrary is derived from the mRNA of an intestinal epithelial cell. ThecDNA libraries are then screened by incubating cells from the librarywith a fluorescent cholesterol absorption inhibitor, and identifyingthose cells that display the greatest amount of fluorescence, using, forexample, fluorescence activated cell sorting (FACS). The cDNA expressedin that cell can then be identified using known techniques.

D. Methods of Screening for Inhibitory Agents

New cholesterol absorption inhibitory agents are screened using methodsof the invention. In general, a substrate is employed which mimics theprotein's natural substrate, but which provides a quantifiable signalwhen bound. The signal is preferably detectable by colorimetric orfluorometric means: however, other methods such as HPLC or silica gelchromatography, GC-MS, nuclear magnetic resonance, and the like may alsobe useful. After optimum substrate and protein (or membrane or cell)concentrations are determined, a candidate inhibitory agent is added tothe reaction mixture at a range of concentrations. The assay conditionsideally should resemble the conditions under which cholesterolabsorption is to be inhibited in vivo, i.e., under physiologic pH,temperature, ionic strength, etc. Suitable inhibitors will exhibitabsorption inhibition at concentrations which do not raise toxic sideeffects in the subject. Inhibitors which compete for binding may requireconcentrations equal to or greater than the substrate concentration,while inhibitors capable of binding irreversibly to the cholesterolbinding site may be added in concentrations on the order of the proteinconcentration.

This invention provides several methods for assaying, identifying orscreening inhibitory agents for activity against cholesterol absorption,including cellular techniques, membrane techniques, and techniques usingproteins that are involved in cholesterol absorption, such as the oneprovided by the current invention, the scavenger receptor type B, classI (SR-BI). SR-BI was first described by Acton et al., J. Biol. Chem.(1994) 269:21003-21009. Screening for inhibitory agents is accomplishedas described below.

In the cellular method, cells capable of binding a fluorescentcholesterol absorption inhibitor are used. In a preferred embodiment,the cells are involved in cholesterol absorption in a biological system.The cells are contacted with candidate inhibitory agents in the presenceof the fluorescent cholesterol absorption inhibitor; the inhibition ofthe fluorescence of said cells are measured.

In the membrane method, a membrane capable of absorbing cholesterol isused. In a preferred embodiment of this invention, the membranes arefrom the intestinal brush border. The membranes are contacted withcandidate inhibitory agents in the presence of the fluorescentcholesterol absorption inhibitor; and the relative presence or absenceof fluorescent cholesterol absorption inhibitor absorption bound to themembrane is measured. A relative absence of fluorescent cholesterolabsorption inhibitor absorption indicates that said candidate inhibitoryagent is an inhibitory agent which inhibits cholesterol absorption intothe membrane.

In the protein method, a cell expressing the scavenger receptor type B,class I (SR-BI) is used. The cell is contacted with a labeledcholesterol absorption inhibitor and a candidate inhibitory agent underconditions wherein, but for the presence of said inhibitory agent, thelabeled cholesterol absorption inhibitor binds to SR-BI, and therelative presence or absence of labeled cholesterol absorption inhibitorabsorption bound to SR-BI is detected. A relative absence of labeledcholesterol absorption inhibitor absorption indicates that the candidateinhibitory agent is an inhibitory agent which inhibits SR-BI-mediatedcellular cholesterol absorption.

The methods of assaying or selecting inhibitory agents of this inventionuse labeled cholesterol absorption inhibitors. The inhibitors themselvesare described in section A, above. The labels used in the assays ofinvention can be primary labels (where the label comprises an elementwhich is detected directly) or secondary labels (where the detectedlabel binds to a primary label, e.g., as is common in immunologicallabeling). An introduction to labels, labeling procedures and detectionof labels is found in Polak and Van Noorden (1997) Introduction toImmunocytochemistry, second edition, Springer Verlag, N.Y. and inHaugland (1996) Handbook of Fluorescent Probes and Research Chemicals, acombined handbook and catalogue Published by Molecular Probes, Inc.,Eugene, Oreg. Primary and secondary labels can include undetectedelements as well as detected elements. Useful primary and secondarylabels in the present invention can include spectral labels, whichinclude fluorescent labels such as fluorescent dyes (e.g., fluoresceinand derivatives such as fluorescein isothiocyanate (FITC) and OregonGreen™, rhodamine and derivatives (e.g., Texas red, tetramethylrhodamineisothiocyanate (TRITC), etc.), digoxigenin, biotin, phycoerythrin, AMCA,CyDyes™, and the like), radiolabels (e.g., ³H, ¹²⁵I, ³⁵S, ¹⁴C, ³²P, ³³p,etc.), enzymes (e.g., horseradish peroxidase, alkaline phosphatase etc.)spectral colorimetric labels such as colloidal gold or colored glass orplastic (e.g. polystyrene, polypropylene, latex, etc.) beads. The labelmay be coupled directly or indirectly to the cholesterol absorptioninhibitor according to methods well known in the art. As indicatedabove, a wide variety of labels may be used, with the choice of labeldepending on sensitivity required, ease of conjugation with thecompound, stability requirements, available instrumentation, anddisposal provisions. In general, a detector which monitors aprotein/inhibitory agent interaction is adapted to the particular labelwhich is used. Typical detectors include spectrophotometers, phototubesand photodiodes, microscopes, scintillation counters, cameras, film andthe like, as well as combinations thereof. Examples of suitabledetectors are widely available from a variety of commercial sourcesknown to persons of skill.

Preferred labels include those which utilize 1) chemiluminescence (usinghorseradish peroxidase or alkaline phosphatase with substrates thatproduce photons as breakdown products) with kits being available, e.g.,from Molecular Probes, Amersham, Boehringer-Mannheim, and LifeTechnologies/Gibco BRL; 2) color production (using both horseradishperoxidase or alkaline phosphatase with substrates that produce acolored precipitate) (kits available from Life Technologies/Gibco BRL,and Boehringer-Mannheim); 3) fluorescence (e.g., using Cy-5 (Amersham),fluorescein, and other fluorescent tags); 5) radioactivity. Othermethods for labeling and detection will be readily apparent to oneskilled in the art.

Fluorescent labels are highly preferred labels, having the advantage ofrequiring fewer precautions in handling, and being amendable tohigh-throughput visualization techniques (optical analysis includingdigitization of the image for analysis in an integrated systemcomprising a computer). Preferred labels are typically characterized byone or more of the following: high sensitivity, high stability, lowbackground, low environmental sensitivity and high specificity inlabeling. Fluorescent moieties, which are incorporated into the labelsof the invention, are generally are known, including Texas red,digoxigenin, biotin, 1- and 2-aminonaphthalene, p,p′-diaminostilbenes,pyrenes, quaternary phenanthridine salts, 9-aminoacridines,p,p′-diaminobenzophenone imines, anthracenes, oxacarbocyanine,merocyanine, 3-aminoequilenin, perylene, bis-benzoxazole, bis-p-oxazolylbenzene, 1,2-benzophenazin, retinol, bis-3-aminopyridinium salts,hellebrigenin, tetracycline, sterophenol, benzimidazolylphenylamine,2-oxo-3-chromen, indole, xanthen, 7-hyddroxycoumarin, phenoxazine,calicylate, strophanthidin, porphyrins, triarylmethanes, flavin and manyothers. Many fluorescent tags are commercially available from the SIGMAchemical company (Saint Louis, Mo.), Molecular Probes, R&D systems(Minneapolis, Minn.), Pharmacia LKB Biotechnology (Piscataway, N.J.),CLONTECH Laboratories, Inc. (Palo Alto, Calif.), Chem Genes Corp.,Aldrich Chemical Company (Milwaukee, Wis.), Glen Research, Inc., GIBCOBRL Life Technologies, Inc. (Gaithersberg, Md.), Fluka ChemicaBiochemikaAnalytika (Fluka Chemie AG, Buchs, Switzerland), and Applied Biosystems(Foster City, Calif.), as well as many other commercial sources known toone of skill.

The labels are covalently bound to the novel cholesterol inhibitors ofthe invention by a tether group. The tether group can be any moietycapable of covalently linking to the inhibitors and to the labels.Preferred groups are substituted or unsusbstituted alkylene, alkenyleneor alkynylene of 1 to 10 carbon atoms, more preferably 1 to 4 carbonatoms. Particularly preferred groups are unsusbstituted alkynylenes.

The candidate and actual inhibitory agents of this invention willpreferably take the form of organic compounds, particularly compoundswhich inhibit the absorption of cholesterol mediated by SR-BI and otherproteins3. Other inhibitory agents may be proteins, particularlyantibodies and antibody derivatives. Recombinant expression systems maybe used to generate quantities of SR-BI sufficient for production ofmonoclonal antibodies (MAbs) specific for SR-BI. Suitable antibodies forcholesterol absorption inhibition will bind to SR-BI in a mannerreducing or eliminating the cholesterol binding activity, typically byobscuring the binding site. Suitable MAbs may be used to generatederivatives, such as Fab fragments, chimeric antibodies, alteredantibodies, univalent antibodies, and single domain antibodies, usingmethods known in the art.

EXAMPLES EXAMPLE 1 A. PREPARATION OF6-(6-HYDROXY-3-OXO-3H-XANTHEN-9-YL)-N-(5-PROP-2-YNYLCARBAMOYL-PENTYL)-ISOPHTHALAMICACID (1)

Added propargyl amine (5 μL,˜4 mg, 73 μmol) to 0.3 mL DMF containing 3-5drops 0.2M aqueous NaHCO,₃then added6-(Fluorescein-5-carboxamido)hexanoic acid, succinimidyl ester (5-SFX;Molecular Probes, Inc.) (5 mg, 8.5 μmol) to the mixture. Stirred thebright orange solution for 3 h at room temperature. Concentrated invacuo and chromatographed the residue over ˜5 g of silica gel elutingwith 10% MeOH in dichloromethane to give the desired terminal alkyne (1)as a yellow brown fluorescent oil. calcd m/z for C₃₀H₂₇N₂O₇=527; foundm/z=527.

B. PREPARATION OF1-O-[4-[TRANS-(3R,4S)-1-[4-[3-[[6-[[[3-CARBOXY-4-(6-HYDROXY-3-OXO-3H-XANTHEN-9-YL)PHENYL]CARBONYL]AMINO]-1-OXOHEXYL]AMINO]-1-PROPENYL]PHENYL]-3-[3-(S)-HYDROXY-3-(4-FLUOROPHENYL)PROPYL]-2-OXO4-AZETIDINYL]PHENYL]-BETA-D-GLUCORONICACID (IB)

To the iodophenylazetidinone glucuronide methyl ester IIIA (disclosed inPat. No. 5756,470, May 26, 1998)( 6.7 mg, 9.47 μmol) in 0.8 mL DMF, wasadded the alkyne (1) (14.8 mg, 28 μmol). Bubbled argon through thereaction mixture, then added palladium tetrakistriphenylphosphine (1.4mg, 1.2 μmol), copper(I) iodide (0.8 mg, 4.2 μmol), and triethylamine (8μL, 57 μmol). Stirred the reaction mixture overnight under argon.Concentrated the reaction onto a prep TLC plate and eluted with 25% MeOHin dichloromethane. Collected the major fluorescent band and purifiedfurther by reverse phase HPLC over aC-18 column eluting with 10-100%acetonitrile in water affording the desired fluorescent methyl ester asan orange solid. FABMS: calcd m/z for C₆₁H₅₇N₃FO₁₆ (M+1)⁺1106.4; foundm/z=1106.5.

The glucuronide methyl ester was then hydrolyzed by dissolving 9 mg ofthe compound in 2 mL of a 7:2:1 mixture of water:triethylamine: methanoland stirring for 1 h. Evaporation to dryness gave the desiredfluorescent azetidinone glucuronide, (IB) as an orange solid. ES-MS:calcd m/z for C₆₀H₅₅N₃FO₁₆ (M+1)⁺=1092.3; found m/z=-1092.3.

Example 2 A. PREPARATION OF4,4-DIFLUORO-5,7-DIMETHYL4-BORA-3a,4a-DIAZA-s-INDACENE-3-N-PROP-2-YNYL-PROPIONAMIDE(2)

To propargyl amine (8 μL, ˜6.4 mg, -117 μmol) in 0.5mL DMF and 1 drop of0.1M NaHCO3, was added4,4-difluoro-5,7-dimethyl4-bora-3a,4a-diaza-s-indacene-3-propionic acid,succinimide ester (BODIPY FL, SE; Molecular Probes, In.) (10 mg, 25.7μmol) in 0.1mL DMF. Stirred the reaction at room temperature for 12 h.Concentrated the mixture in vacuo and chromatographed the residue over˜5 g silica gel eluting with 1% MeOH in dichloromethane to give thedesired alkyne (2) as a yellow orange oil. R_(f)=0.62 in 5% MeOH inCH₂Cl₂ on SiO₂ TLC.

B. PREPARATION OF[1-O-[4-[1-[4-[3-[[3-[2-[(3,5-DIMETHYL-1H-PYRROL-2-YL-.KAPPA.N)METHYLENE]-2H-PYRROL-5-YL-.KAPPA.N]-1-OXOPROPYL]AMINO]-1-PROPYNYL]PHENYL]-3(R)-[3(S)-HYDROXY-3-(4-FLUOROPHENYL)PROPYL]-2-OXO-4(S)-AZETIDINYL]PHENYL]-BETA-D-GLUCURONATO]DIFLUOROBORATE,HYDROGEN (IC)

To the iodophenylazetidinone glucuronide methyl ester IIIA (disclosed inPat. No. 5756,470 May 26, 1998) (7.7 mg, 10.9 μmol) in 1 mL DMF, wasadded (7.2 mg, 10.9 μmol) of the BODIPY alkyne (2). Bubbled argonthrough the solution for a few minutes and then added palladiumtetrakistriphenylphosphine (1.2 mg, 1 μmol), copper(I) iodide (0.6 mg, 3μmol), and triethylamine (10 μL, 7 μmol). Stirred the reaction overnightunder argon. Removed the solvent in vacuo and purified the product viaprep TLC eluting with a 50:50:17:1 mixture of ethylacetate:hexanes:methanol:acetic acid to give the desired fluorescentmethyl ester as an orange solid. ESI-MS: calcd m/z for C₄₈H₄₉BF₃N₄O₁₀(M+1)⁺=909.3; found m/z=909.2.

The glucuronide methyl ester was then hydrolyzed by dissolving 4.2 mg ofthe compound in ˜1 mL of a 7:2:1 mixture of water:triethylamine:methanol and stirring for 1 h. Evaporation to dryness gave the desiredfluorescent azetidinone glucuronide (IC) as an orange solid, ES-MS:calcd m/z for C₄₇H₄₆BF₂N₄O₁₀ (M+1−HF)⁺=875.3; found m/z=875.3.

Example 3 DETERMINATION OF CHOLESTEROL ABSORPTION INHIBITORY ACTIVITY

Male Sprague-Dawley rats weighing 300-400 g were used. After anovernight fast, rats were anesthetized (Inactin, 0.1 mg/kg i.p.) for theduration of each study and were fitted with a cannula into the smallintestine just below the pyloric valve. For the cannulation of the smallintestine, a catheter (Surflo® i.v. catheter (18GX2″), Terumo MedicalCorporation; Elkton, Md.) was inserted through the fundus of thestomach, advanced 1 cm beyond the pylorus, and ligated in place.Compounds were mixed in rat bile and delivered by bolus injection (1 mL)via the intestinal catheter into the small intestine.

One hour after the bile doses were delivered, three mL of an emulsionconsisting of 2.23 mg/mL L-phosphatidylcholine and 11.8 mg/mL trioleinin 19 mM sodium taurocholate (Sigma; St. Louis, Mo.) buffer (pH 6.4)containing 3 mg cholesterol and 1 mCi ¹⁴C-cholesterol (NEN; Boston,Mass.) was delivered to each rat as a bolus via the intestinal cannula.Ninety minutes after the cholesterol emulsion was delivered, the ratswere euthanized. Blood was collected and plasma was separated bycentrifugation at 2000 rpm for 15 min at 4° C. Triplicate aliquots ofplasma were analyzed ¹⁴C radioactivity and inhibition of cholesterolabsorption relative to bile vehicle control rats was determined.

The ID50 for IIA in this acute model of cholesterol absorption wascalculated to be 0.0015 mg/kg (Van Heek, M., France, C. F., Compton, D.S., McLeod, R. L., Yumibe, N. P., Alton, K. B., Sybertz, E. J., andDavis, H. R.: In vivo mechanism-based discovery of a potent cholesterolabsorption inhibitor (IIA) through the identification of the activemetabolites of IVA. The Journal of Pharmacology and ExperimentalTherapeutics (JPET), 283: 157-163, 1997). TABLE 1 In Vivo CholesterolAbsorption Activity: % Inhibition of [14C]-Cholesterol Compound # Dose(μg/kg) Absorption into Plasma IA 10 91% IB 56 79% IB 186 88% 1C 30 58%1C 100 80%IA is the glucuronide of IIA

Example 4 IDENTIFICATION OF PROTEINS INVOLVED IN CHOLESTEROL ABSORPTIONAND TRAFFICKING; EXPRESSION CLONING EXPERIMENTS

The small intestine was removed from male CRL: CD BR rats. Intestinalepithelial cells were isolated by the method of Weiser (Weiser, M.,1973, JBC 248, 2536-2541) and the mRNA extracted. Poly A mRNA waspurified and double stranded cDNA synthesized. Adapter linkers wereligated followed by size selection (>2 Kb) of the cDNA. The selectedfraction of cDNA was ligated into the retroviral expression plasmid pMX,subsequently transformed into bacteria and grown on selective agar at aclonal density of −30,000/plate. Each pool of bacterial clones wascollected and plasmid DNA prepared.

Individual pools of cDNA library were transformed into the retroviralpackaging cell line BOSC23 and the resulting viral particles, containingthe cDNA library, were used to infect the mouse cell line BW5147.Following infection BW5147 cells were stained with compound 1C andanalyzed by fluorescent activated cell sorting (FACS). Positive stainingcells (−01%) were recovered and re-cultured. The process of recoveringpositive staining cells was repeated after expansion of the cellpopulation in culture and following the second round of FACS analysisindividual cells were isolated by limiting dilution.

Individual clonal populations of cells were subjected to PCR usingretroviral vector specific oligonucleotide primers designed to flank themultiple cloning site in which the cDNA library was cloned. ResultingDNA fragments were subcloned and completely sequenced to determine theidentification of the cloned cDNA. By sequencing two clones isolatedfrom two independent cDNA expression libraries, Scavenger receptor,class B, type I (SR-BI) (GENBANK Accession Numbers: U76205 —submissiondate Oct. 24, 1996; D89655—submission date Dec. 3, 1996, andAB002151—submission date Mar. 26, 1997) was identified as the cellularreceptor for compound IC.

The above described method may be used in conjunction with any of theazetidinone compounds referred to herein to identify other proteins thatare involved in cholesterol absorption or trafficking.

Once identified, further characterization of the proteins can beconducted, for example, using the following methods:

(1) FACS analysis of target expressing cells with fluorescent compoundbinding can be utilized in both direct and competition binding formats.Added complexity by the addition of other cellularly expressed proteinsas well as the addition of exogenous molecules such as antibodies andother soluble factors can also be examined; and

(2) Equilibrium and competition binding can be conducted in similarfashion to radiolabeled ligand analysis by simply substituting afluorescent spectrophotometer for a scintillation counter and measuringcell associated fluorescence instead of radioactivity.

1-28. (canceled)
 29. An isolated cell wherein a fluorescent cholesterol absorption inhibitor is bound to a surface of said cell, wherein said inhibitor is an azetidinone.
 30. The cell of claim 29 wherein said inhibitor is represented by structural formula I or II:

wherein R is a fluorescent moiety.
 31. The cell of claim 30 wherein R is linked to the fluorescent moiety by an alkynyl containing tethering group.
 32. The cell of claim 31 wherein R is represented by a structural formula selected from the group consisting of:


33. The cell of claim 29 which comprises a cDNA library.
 34. The cell of claim 29 which is a BW5147 cell. 